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Review
. 2024 Sep 26:15:1464803.
doi: 10.3389/fendo.2024.1464803. eCollection 2024.

Primary ovarian insufficiency: update on clinical and genetic findings

Affiliations
Review

Primary ovarian insufficiency: update on clinical and genetic findings

Silvia Federici et al. Front Endocrinol (Lausanne). .

Abstract

Primary ovarian insufficiency (POI) is a disorder of insufficient ovarian follicle function before the age of 40 years with an estimated prevalence of 3.7% worldwide. Its relevance is emerging due to the increasing number of women desiring conception late or beyond the third decade of their lives. POI clinical presentation is extremely heterogeneous with a possible exordium as primary amenorrhea due to ovarian dysgenesis or with a secondary amenorrhea due to different congenital or acquired abnormalities. POI significantly impacts non only on the fertility prospect of the affected women but also on their general, psychological, sexual quality of life, and, furthermore, on their long-term bone, cardiovascular, and cognitive health. In several cases the underlying cause of POI remains unknown and, thus, these forms are still classified as idiopathic. However, we now know the age of menopause is an inheritable trait and POI has a strong genetic background. This is confirmed by the existence of several candidate genes, experimental and natural models. The most common genetic contributors to POI are the X chromosome-linked defects. Moreover, the variable expressivity of POI defect suggests it can be considered as a multifactorial or oligogenic defect. Here, we present an updated review on clinical findings and on the principal X-linked and autosomal genes involved in syndromic and non-syndromic forms of POI. We also provide current information on the management of the premature hypoestrogenic state as well as on fertility preservation in subjects at risk of POI.

Keywords: estradiol; estradiol replacement therapy; female hypogonadism; premature menopause; premature ovarian failure.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer AC declared a shared affiliation with the authors to the handling editor at the time of review. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Figures

Figure 1
Figure 1
Schematic illustration of the genetic candidates for POI, according to the biological process of Meiotic Prophase I (A) and Folliculogenesis (B) and based on literature findings. PGCs, Primordial Germ Cells; PmFs, Primordial Follicles; PrFs, Primary Follicles; SFs, Secondary Follicles; Afs, Antral Follicles; GFs, Graafian Follicles. Figure created with Biorender.com.

References

    1. Nelson LM. Clinical practice. Primary ovarian insufficiency. N Engl J Med. (2009) 360:606–14. doi: 10.1056/NEJMcp0808697 - DOI - PMC - PubMed
    1. Stuenkel CA, Gompel A. Primary ovarian insufficiency. N Engl J Med. (2023) 388:154–63. doi: 10.1056/NEJMcp2116488 - DOI - PubMed
    1. Welt CK. Primary ovarian insufficiency: a more accurate term for premature ovarian failure. Clin Endocrinol (Oxf). (2008) 68:499–509. doi: 10.1111/j.1365-2265.2007.03073.x - DOI - PubMed
    1. Huhtaniemi I, Hovatta O, La Marca A, Livera G, Monniaux D, Persani L, et al. . Advances in the molecular pathophysiology, genetics, and treatment of primary ovarian insufficiency. Trends Endocrinol Metab. (2018) 29:400–19. doi: 10.1016/j.tem.2018.03.010 - DOI - PubMed
    1. Rossetti R, Ferrari I, Bonomi M, Persani L. Genetics of primary ovarian insufficiency. Clin Genet. (2017) 91:183–98. doi: 10.1111/cge.12921 - DOI - PubMed

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